A ratiometric fluorescent probe for cysteine and glutathione differentiation and its application for cysteine detection in foods

被引:0
|
作者
You, Wenhui [1 ,2 ]
Huang, Shumei [1 ,2 ]
Chen, Gang [1 ,2 ]
Lin, Zhenxin [1 ,2 ]
Jiang, Yin [1 ,2 ]
Qian, Jiang [3 ]
Zhang, Huatang [1 ,2 ,4 ]
Sun, Hongyan [5 ,6 ,7 ]
机构
[1] Guangdong Univ Technol, Sch Chem Engn & Light Ind, Guangzhou, Guangdong, Peoples R China
[2] Guangdong Univ Technol, Sch Biomed & Pharmaceut Sci, Guangzhou, Guangdong, Peoples R China
[3] Sun Yat Sen Univ, Zhongshan Sch Med, Guangzhou, Guangdong, Peoples R China
[4] Jieyang Ctr, Guangdong Lab Chem & Fine Chem Ind, Jieyang 522000, Guangdong, Peoples R China
[5] City Univ Hong Kong, Shenzhen Res Inst, Shenzhen 518057, Peoples R China
[6] City Univ Hong Kong, Dept Chem, Kowloon, 83 Tat Chee Ave, Hong Kong, Peoples R China
[7] City Univ Hong Kong, COSDAF Ctr Superdiamond & Adv Films, 83 Tat Chee Ave, Hong Kong, Peoples R China
基金
中国国家自然科学基金;
关键词
Fluorescent probe; Cysteine; Glutathione; N-terminal Cys; SELECTIVE DETECTION;
D O I
10.1016/j.molstruc.2024.138852
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Cysteine (Cys) and glutathione (GSH) are crucial biothiols implicated in cellular redox balance, necessitating accurate detection methods. Herein, we developed a novel fluorescent probe based on the fluorescent dye pyronin (PYR), capable of monitoring both Cys-and GSH using ratiometric fluorescence signals. The probe, named PYR-CG, where "C" stands for Cys-and "G" stands for GSH, demonstrates selective detection capabilities for Cys-and GSH. UV absorption and fluorescence emission spectra changes revealed distinct shifts upon interaction with Cys-and GSH. Theoretical and experimental studies validated PYR-CG's responsiveness to Cys-and GSH, elucidating its mechanism as a ratiometric probe. Notably, PYR-CG exhibited rapid response kinetics for Cys-and GSH, with low detection limits of 88 nM and 164 nM, respectively. Importantly, PYR-CG demonstrated exceptional selectivity for Cys-and GSH over interfering analytes. Screening of molecules with similar structures to Cys-further affirmed PYR-CG's specificity, particularly towards N-terminal Cys-in peptides. Furthermore, recovery experiments underscored PYR-CG's reliability for quantitative Cys-detection in complex food samples. Our findings highlight the innovative design and practical applicability of PYR-CG, offering a valuable tool for sensitive and selective detection of Cys-in diverse biological and food samples.
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